Description

Clofeverine is a synthetic organic compound with specific pharmacological activity, widely recognized in the research and development of therapeutic agents. This compound is valued for its role as a key intermediate or active pharmaceutical ingredient (API) in the synthesis of specialized medications. It is primarily sought by pharmaceutical manufacturers, biotechnology research firms, and academic institutions engaged in drug discovery and advanced chemical synthesis.

Application

• Pharmaceutical Intermediate: Serves as a critical building block in the multi-step synthesis of target drug molecules.
• Active Pharmaceutical Ingredient (API) Research: Used in preclinical and clinical research for developing new therapeutic formulations.
• Biochemical Research: Employed in laboratory studies to investigate biological pathways and mechanisms of action.
• Reference Standard: Utilized as a high-purity standard in analytical testing (HPLC, GC) for quality control and method validation.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.

Basic Information

Product Name	Clofeverine
CAS No.	54340-63-5
Molecular Formula	C20H24ClNO3
Molecular Weight	361.86 g/mol
Synonyms	Clofeverine; 2-[4-(2-Chlorophenyl)phenyl]-N,N-diethylacetamide; 4'-(2-Chloro[1,1'-biphenyl]-4-yl)-N,N-diethylacetamide; Clofeverin; L-9394; McN-JR-6218; McNJR-6218
EINECS	Contact for details

Quality Control

Our Clofeverine is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure high purity and consistency, meeting the stringent requirements for pharmaceutical research and development. Certificates of Analysis (COA) detailing purity, identity, and impurity profiles are provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.